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Total synthesis of amphotericin B. 3. The final stages

Journal of the American Chemical Society, 1988-07, Vol.110 (14), p.4696-4705

1988

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A modern analogue of western United States summer palaeoclimate at 6000 years before present

Holocene (Sevenoaks), 1999-09, Vol.9 (5), p.541-545

1999

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Total synthesis of amphoteronolide B and amphotericin B. 1. Strategy and stereocontrolled construction of key building blocks

Journal of the American Chemical Society, 1988-07, Vol.110 (14), p.4672-4685

1988

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Total synthesis of amphoteronolide B and amphotericin B. 2. Total synthesis of amphoteronolide B

Journal of the American Chemical Society, 1988-07, Vol.110 (14), p.4685-4696

1988

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First X-ray Cocrystal Structure of a Bacterial FabH Condensing Enzyme and a Small Molecule Inhibitor Achieved Using Rational Design and Homology Modeling

Journal of medicinal chemistry, 2003-01, Vol.46 (1), p.5-8

2003

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Identification, substrate specificity, and inhibition of the Streptococcus pneumoniae beta-ketoacyl-acyl carrier protein synthase III (FabH)

The Journal of biological chemistry, 2001-08, Vol.276 (32), p.30024-30030

2001

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Chemistry of amphotericin B. Degradation studies and preparation of amphoteronolide B

Journal of the American Chemical Society, 1988-07, Vol.110 (14), p.4660-4672

1988

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In vitro and in vivo pharmacological characterization of SB 201993, an eicosanoid-like LTB4 receptor antagonist with anti-inflammatory activity

Prostaglandins, leukotrienes and essential fatty acids, 1999-07, Vol.61 (1), p.55-64

1999

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Pharmacology of SB-273779, a nonpeptide calcitonin gene-related peptide 1 receptor antagonist

The Journal of pharmacology and experimental therapeutics, 2001-03, Vol.296 (3), p.768

2001

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Total synthesis of amphotericin B

Journal of the American Chemical Society, 1987-04, Vol.109 (9), p.2821-2822

1987

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Total synthesis of amphoteronolide B

Journal of the American Chemical Society, 1987-04, Vol.109 (7), p.2208-2210

1987

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Stereocontrolled construction of key building blocks for the total synthesis of amphoteronolide B and amphotericin B

Journal of the American Chemical Society, 1987-04, Vol.109 (7), p.2205-2208

1987

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(E)-3-[6-[[(2,6-Dichlorophenyl)thio]methyl]-3-(2-phenylethoxy)-2-pyridinyl]-2- propenoic Acid: A High-Affinity Leukotriene B4 Receptor Antagonist with Oral Antiinflammatory Activity

Journal of medicinal chemistry, 1996-09, Vol.39 (19), p.3837-3841

1996

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Crystal structure and substrate specificity of the β‐ketoacyl‐acyl carrier protein synthase III (FabH) from Staphylococcus aureus

Protein science, 2005-08, Vol.14 (8), p.2087-2094

2005

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Quinine analogs as non-peptide calcitonin gene-related peptide (CGRP) receptor antagonists

Bioorganic & medicinal chemistry letters, 1997-10, Vol.7 (20), p.2673-2676

1997

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Synthesis of structural analogs of leukotriene B4 and their receptor binding activity

Journal of medicinal chemistry, 1993-10, Vol.36 (22), p.3308-3320

1993

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Trisubstituted pyridine leukotriene B4 receptor antagonists: synthesis and structure-activity relationships

Journal of medicinal chemistry, 1993-10, Vol.36 (22), p.3321-3332

1993

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(E)-3-[[[[6-(2-Carboxyethenyl)-5-[[8-(4-methoxyphenyl)octyl]oxy]-2-pyridinyl]methyl]thio]methyl]benzoic acid: a novel high-affinity leukotriene B4 receptor antagonist

Journal of medicinal chemistry, 1993-09, Vol.36 (18), p.2703-2705

1993

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Bacterial beta-ketoacyl-acyl carrier protein synthases as targets for antibacterial agents

Current protein & peptide science, 2003-02, Vol.4 (1), p.21-29

2003

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Retrosynthetic and synthetic chemistry on amphotericin B. Synthesis of C(1)―C(20) and C(21)―C(38) fragments and construction of the 38-membered macrocycle

Journal of the Chemical Society. Chemical communications, 1986 (5), p.413-416

1986

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Amphoteronolide B methyl ester. Novel oxidative deglycosidation of amphotericin B

Journal of the Chemical Society. Chemical communications, 1987 (9), p.686-689

1987

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SB 209247, a high affinity LTB4 receptor antagonist demonstrating potent antiinflammatory activity

Advances in prostaglandin, thromboxane, and leukotriene research, 1995, Vol.23, p.275

1995

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(E)-3-[[[[6-(2-Carboxyethenyl)-5-[[8-(4-methoxyphenyl)octyl]oxy]-2-pyridinyl]methyl]thio]methyl]benzoic Acid and Related Compounds: High Affinity Leukotriene B4 Receptor Antagonists

Journal of medicinal chemistry, 1994-09, Vol.37 (20), p.3327-3336

1994

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( E )-3-[6-[[(2,6-Dichlorophenyl)thio]methyl]-3-(2-phenylethoxy)-2-pyridinyl]-2- propenoic Acid: A High-Affinity Leukotriene B 4 Receptor Antagonist with Oral Antiinflammatory Activity

Journal of medicinal chemistry, 1996-09, Vol.39 (19), p.3837-3841

1996

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(E)-3-[[[[6-(2-carboxyethenyl)-5-[[8-(4-methoxyphenyl)octyl]oxy]-2-pyridinyl]-methyl]thio]benzoic acid and related compounds : high affinity leukotriene B4 receptor antagonists

Journal of medicinal chemistry, 1994, Vol.37 (20), p.3327-3336

1994

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Total synthesis of amphotericin B. 3. The final stages

A modern analogue of western United States summer palaeoclimate at 6000 years before present

Total synthesis of amphoteronolide B and amphotericin B. 1. Strategy and stereocontrolled construction of key building blocks

Total synthesis of amphoteronolide B and amphotericin B. 2. Total synthesis of amphoteronolide B

First X-ray Cocrystal Structure of a Bacterial FabH Condensing Enzyme and a Small Molecule Inhibitor Achieved Using Rational Design and Homology Modeling

Identification, substrate specificity, and inhibition of the Streptococcus pneumoniae beta-ketoacyl-acyl carrier protein synthase III (FabH)

Chemistry of amphotericin B. Degradation studies and preparation of amphoteronolide B

In vitro and in vivo pharmacological characterization of SB 201993, an eicosanoid-like LTB4 receptor antagonist with anti-inflammatory activity

Pharmacology of SB-273779, a nonpeptide calcitonin gene-related peptide 1 receptor antagonist

Total synthesis of amphotericin B

Total synthesis of amphoteronolide B

Stereocontrolled construction of key building blocks for the total synthesis of amphoteronolide B and amphotericin B

(E)-3-[6-[[(2,6-Dichlorophenyl)thio]methyl]-3-(2-phenylethoxy)-2-pyridinyl]-2- propenoic Acid: A High-Affinity Leukotriene B4 Receptor Antagonist with Oral Antiinflammatory Activity

Crystal structure and substrate specificity of the β‐ketoacyl‐acyl carrier protein synthase III (FabH) from Staphylococcus aureus

Quinine analogs as non-peptide calcitonin gene-related peptide (CGRP) receptor antagonists

Synthesis of structural analogs of leukotriene B4 and their receptor binding activity

Trisubstituted pyridine leukotriene B4 receptor antagonists: synthesis and structure-activity relationships

(E)-3-[[[[6-(2-Carboxyethenyl)-5-[[8-(4-methoxyphenyl)octyl]oxy]-2-pyridinyl]methyl]thio]methyl]benzoic acid: a novel high-affinity leukotriene B4 receptor antagonist

Bacterial beta-ketoacyl-acyl carrier protein synthases as targets for antibacterial agents

Retrosynthetic and synthetic chemistry on amphotericin B. Synthesis of C(1)―C(20) and C(21)―C(38) fragments and construction of the 38-membered macrocycle

Amphoteronolide B methyl ester. Novel oxidative deglycosidation of amphotericin B

SB 209247, a high affinity LTB4 receptor antagonist demonstrating potent antiinflammatory activity

(E)-3-[[[[6-(2-Carboxyethenyl)-5-[[8-(4-methoxyphenyl)octyl]oxy]-2-pyridinyl]methyl]thio]methyl]benzoic Acid and Related Compounds: High Affinity Leukotriene B4 Receptor Antagonists

( E )-3-[6-[[(2,6-Dichlorophenyl)thio]methyl]-3-(2-phenylethoxy)-2-pyridinyl]-2- propenoic Acid: A High-Affinity Leukotriene B 4 Receptor Antagonist with Oral Antiinflammatory Activity

(E)-3-[[[[6-(2-carboxyethenyl)-5-[[8-(4-methoxyphenyl)octyl]oxy]-2-pyridinyl]-methyl]thio]benzoic acid and related compounds : high affinity leukotriene B4 receptor antagonists

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